ENST00000261937.11:c.3936C>T
MANE Select
|
ENSP00000261937.6:p.His1312=
|
|
ENST00000261937.10:c.3936C>T
|
ENSP00000261937.6:p.His1312=
|
|
ENST00000502603.5:n.636C>T
|
|
|
NM_182925.4:c.3936C>T
|
NP_891555.2:p.His1312=
|
|
XM_011534477.1:c.4185C>T
|
XP_011532779.1:p.His1395=
|
|
XM_011534478.1:c.4167C>T
|
XP_011532780.1:p.His1389=
|
|
XM_011534479.1:c.*82C>T
|
XP_011532781.1:n.*82C>T
|
|
XM_011534482.1:c.3954C>T
|
XP_011532784.1:p.His1318=
|
|
XM_011534483.1:c.3876C>T
|
XP_011532785.1:p.His1292=
|
|
XM_011534484.1:c.3477C>T
|
XP_011532786.1:p.His1159=
|
|
XR_941095.1:n.4222C>T
|
|
|
XM_011534478.3:c.4167C>T
|
XP_011532780.1:p.His1389=
|
|
XM_011534484.2:c.3477C>T
|
XP_011532786.1:p.His1159=
|
|
XM_017009263.1:c.*82C>T
|
XP_016864752.1:n.*82C>T
|
|
XM_017009268.1:c.3858C>T
|
XP_016864757.1:p.His1286=
|
|
XR_001742050.2:n.4426C>T
|
|
|
NM_182925.5:c.3936C>T
MANE Select
|
NP_891555.2:p.His1312=
|
|